首页> 外文期刊>Journal of Clinical Oncology >Efficacy of sequential high-dose doxorubicin and ifosfamide compared with standard-dose doxorubicin in patients with advanced soft tissue sarcoma: an open-label randomized phase ii study of the spanish group for research on sarcomas.
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Efficacy of sequential high-dose doxorubicin and ifosfamide compared with standard-dose doxorubicin in patients with advanced soft tissue sarcoma: an open-label randomized phase ii study of the spanish group for research on sarcomas.

机译:序贯大剂量阿霉素和异环磷酰胺与标准剂量阿霉素相比在晚期软组织肉瘤患者中的疗效:西班牙组用于肉瘤研究的开放标签随机ii期研究。

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PURPOSE: To assess the progression-free survival (PFS) and antitumor response to standard-dose doxorubicin compared with sequential dose-dense doxorubicin and ifosfamide in first-line treatment of advanced soft tissue sarcoma. PATIENTS AND METHODS: Patients with measurable advanced soft tissue sarcoma, Eastern Cooperative Oncology Group (ECOG) performance status (PS) < 2, between the ages 18 and 65 years, and with adequate bone marrow, liver, and renal function were entered in the study. The stratifications were: ECOG PS (0 v 1), location of metastases, and potentially resectable disease. Patients were randomly assigned to either doxorubicin 75 mg/m(2) given as a bolus injection every 3 weeks for 6 cycles (arm A) or doxorubicin at 30 mg/m(2) per day for 3 consecutive days once every 2 weeks for 3 cycles followed by ifosfamide at 12.5 g/m(2) delivered by continuous infusion over 5 days once every 3 weeks for 3 cycles with filgastrim or pegfilgastrim support (arm B). RESULTS: Between December 2003 and September 2007, 132 patients were entered onto the study. Febrile neutropenia, asthenia, and mucositis were more frequent in the arm B. The interim preplanned analysis for futility allowed the premature closure. Objective responses were observed in 23.4% of assessable patients in arm A and 24.1% in arm B. PFS was 26 weeks in the arm A and 24 weeks in arm B (P = .88). Overall survival did not differ between the two therapeutic arms (P = .14). CONCLUSION: Single-agent doxorubicin remains the standard treatment in fit patients with advanced soft tissue sarcoma.
机译:目的:评估一线治疗晚期软组织肉瘤与标准剂量多柔比星和异环磷酰胺相比,对标准剂量阿霉素的无进展生存期(PFS)和抗肿瘤反应。患者和方法:将年龄在18至65岁之间,可测量的晚期软组织肉瘤,东部合作肿瘤小组(ECOG)的表现状态(PS)<2,并且具有足够的骨髓,肝和肾功能的患者纳入研究。研究。分层为:ECOG PS(0 v 1),转移部位和潜在可切除的疾病。患者被随机分配为每3周推注一次的阿霉素75 mg / m(2),共6个周期(A组),或以每天30 mg / m(2)的阿霉素的剂量连续3天,每2周一次3个周期,然后以12.5 g / m(2)的异环磷酰胺,每3周一次连续5天连续输注,持续3周期,并用氟来舒定或培非氟辛辅助治疗(B组)。结果:2003年12月至2007年9月,共有132例患者进入研究。 B臂中发热性中性粒细胞减少,乏力和粘膜炎更为常见。临时性针对无效性的预先计划分析允许过早关闭。 A组中23.4%的可评估患者观察到客观反应,B组中24.1%的患者观察到客观反应。A组中PFS为26周,B组为24周(P = .88)。两个治疗组的总生存期无差异(P = 0.14)。结论:阿霉素单药仍然是适合的晚期软组织肉瘤患者的标准治疗方法。

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